Tag | Content |
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EnhancerAtlas ID | HS034-13556 |
Organism | Homo sapiens |
Tissue/cell | ECC-1 |
Coordinate | chr18:12026440-12027810 |
Target genes | |
TF binding sites/motifs | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
SOX10 | MA0442.2 | chr18:12026489-12026500 | AAAACAAAGAC | + | 6.14 |
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| Number of super-enhancer constituents: 8 | ID | Coordinate | Tissue/cell |
SE_23131 | chr18:12026626-12027467 | Colon_Crypt_1 | SE_23828 | chr18:12026526-12027431 | Colon_Crypt_2 | SE_25040 | chr18:12026514-12027554 | Colon_Crypt_3 | SE_26608 | chr18:12026134-12029486 | Esophagus | SE_31757 | chr18:12026579-12027399 | Gastric | SE_47528 | chr18:12026426-12027538 | Pancreas | SE_48386 | chr18:12026479-12029300 | Psoas_Muscle | SE_65647 | chr18:12026302-12027849 | Pancreatic_islets |
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| Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| Number: 1 | ID | Chromosome | Start | End |
GH18I012026 | chr18 | 12026490 | 12028209 |
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Enhancer Sequence | AAACATTTCT CCCATAAATT AAAATACTAG TAATTTAATG AACCAAATCA AAACAAAGAC 60 TCCAATCCTA CCTTCTTGAG CGCTGGCATT TGAGGGAAAG CACTCATTCA TTCAGTAACT 120 GTTTATCGAG TGCCCACTCA GCCTGGGTCT GCTGATGTCT CTTTCTTTAA TGGAAGCCTT 180 CCCCACCCCC ACCCCGGAAA AAATACCATC TGTTTGTGGC CAGGTGAGGG TGGGGTTTGG 240 AGGGTAAGGA ATGGAAGGGT TGCTGGAGCC TGTCTGCAGA TCCTGTGTGG ATTAGGGAGC 300 ACCTGGAACA GCCGCCTTTT GTCCCAGCTG TGGGTGGCAG CTGCAGGGCT CAGGTGGTAT 360 CTGTGGAGGG CCTGCTGCCA GTCCCAGGGC AGGAGTGCCC TCATAGCTCA GCTTCAGTGC 420 TGGGCATGGC CGGCGGTGAA TGATCTGGAC CTCCTGAGGG CAGGCAGGTT GCTTTGGTGT 480 GGAGCCAGGT GTTTTGCAGA AAGTGCTTTA AGGTGTAAAA TGAGAGTTTC CATGGAAGAA 540 AAGGGACACT TGGACCTGGA TTCTGGCTGA GAGATTTCCT GGGTGAGCGG AGAATTTGAA 600 AGTGGTGACA CAGAACTGGG TCCATTGAGT GCAGTAATGT GATAGGATTT GTTTCCCCCG 660 ACTTTGGGAG TGGCTTTATT TTGTCATGGA GCACACCTGG TTTGGCACTG TCCTGCCCGG 720 GCAGTGAGGC CTGACGGGAC ATGACCGAAG TTTGGCTGTG TTTGGGTGTG TGGCACAACA 780 AGGACAAACT GCTCTGATCC CCAGCAGTGA GTCAGGGACA GGAGCAGAAT CCCGGTCACG 840 TCCTGCCCTG AGCCAGGCTT GCCAGCCCTG GCAGCCTCGC CTGCTGTTAC ATAAACGGCA 900 GGCCATGAAT TCCAGGTGTC GGCACCCCCC TGCATCCAGA GGGCTCACTC CTGCAGCTTC 960 CCTTTCCAAA GCAGCATTAT TTAAAAGTTG CTTTCTCCAA GAAAATGGTA TTTCTATCGT 1020 TGCGATTGCA GCAGTTAGAC GATTAATGAA GCATTTTTTC CCTCCAAACA TTGAGTGTTC 1080 CCAGTTTGGA GTCATTTTGC TTTTCTTTTT GGTTGAATGA TGGTGATTTT TTTTTTTTTT 1140 TTTTTTTTTA AAGAAACAGG GACTTGCTCT GTCCTCCAGG CTGGAATGTG GTGGCGCAAT 1200 CATGGCTGAC AGCAGCCTTG AACCCCTGGG CTCAACCAAT CCTCCCACCT CAGCCTCCTG 1260 AGTAGCTGCA ACTACAGGCC TGTGCCACCA TGCCCAGCTA CTTTTAATTT TTTTTTTTTT 1320 TGCAGAGATG GAGTCTCACC ATCTTGCCCA GGCTGGTCTG GAACTCATGG 1370
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